Variant #0001888623 (NC_000021.8:g.43639368G>T, NC_000021.8(NM_207174.1):c.-714G>T (ABCG1))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43639368G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG1_000007
Frequency 1/12948
Freq. EA 1/8568
Freq. AA 0/4380
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:49:50 +02:00 (CEST)
Date last edited 2023-03-29 07:25:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG1 NM_207174.1 ?/? c.-714G>T r.(=) p.(=)